2010
DOI: 10.1016/j.vaccine.2010.04.102
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A goat poxvirus-vectored peste-des-petits-ruminants vaccine induces long-lasting neutralization antibody to high levels in goats and sheep

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Cited by 80 publications
(62 citation statements)
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“…Multivalent vaccines are currently being developed that may both protect vaccinated animals against several viral pathogens and enable vaccinated and infected animals to be distinguished using DIVA tests. Currently, vaccines exist based on the incorporation of PPRV immunogens into vectors such as sheep and goat pox (Berhe et al, 2003;Chaudhary et al, 2009;Chen et al 2010;Diallo et al, 2002) and attempts are also being made to develop new vaccines based on recombinant DNA technology .…”
Section: Pprv: Diagnosis Prevention and Future Controlmentioning
confidence: 99%
“…Multivalent vaccines are currently being developed that may both protect vaccinated animals against several viral pathogens and enable vaccinated and infected animals to be distinguished using DIVA tests. Currently, vaccines exist based on the incorporation of PPRV immunogens into vectors such as sheep and goat pox (Berhe et al, 2003;Chaudhary et al, 2009;Chen et al 2010;Diallo et al, 2002) and attempts are also being made to develop new vaccines based on recombinant DNA technology .…”
Section: Pprv: Diagnosis Prevention and Future Controlmentioning
confidence: 99%
“…This is especially useful in situations where surveillance is being implemented at the same time as vaccination. In recent years several such vaccines have been successfully developed, particularly using adenovirus [52][53][54][55] and goat/ sheep pox vectors [56][57][58], and some have been tested for efficacy in conventional PPR challenge studies; however, their capacity for long-term protection (up to 2 years) has yet to be determined. For vectored vaccines, the presence of pre-existing immunity against the vector, i.e.…”
Section: Development and Application Of Pprv Vaccinesmentioning
confidence: 99%
“…However, DIVA vaccine candidates would need to be evaluated in comparison with conventional vaccines for the full range of vaccine attributes (e.g., efficacy, impact on virus shedding and transmission, duration of immunity, range of protection, safety, minimum dose, ease of production, cost) in addition to diagnostic advantages. Candidate vaccines for DIVA technologies include capripox (30,31) and adenovirusvectored vaccines (18,32). Prior exposure to capripox reduced the immune responses to the PPR Ags in vaccinates and, in the one study where challenge was carried out, incomplete protection against clinical disease.…”
Section: Suitable Vaccines and Diagnostics Are Availablementioning
confidence: 99%